Novel RNA Synthesis Method Using 5‘-O-Silyl-2‘-O-orthoester Protecting Groups-Reference-Cited by-同舟云学术

Novel RNA Synthesis Method Using 5‘-O-Silyl-2‘-O-orthoester Protecting Groups

Published:1998-11-01 Issue:45 Volume:120 Page:11820-11821
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Scaringe Stephen A.¹,Wincott Francine E.¹,Caruthers Marvin H.¹

Affiliation:

1. Dharmacon Research, Inc., Boulder, Colorado 80301 Ribozyme Pharmaceuticals, Inc., Boulder, Colorado 80301 University of Colorado, Boulder, Colorado 80309

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja980730v

Reference24 articles.

1. Tethering Ribozymes to a Retroviral Packaging Signal for Destruction of Viral RNA

2. Exploiting the chemical synthesis of RNA

3. The synthesis of oligoribonucleotides. II. The use of silyl protecting groups in nucleoside and nucleotide chemistry. VII

4. The automated chemical synthesis of long oligoribuncleotides using 2'-O-silylated ribonucleoside 3'-O-phosphoramidites on a controlled-pore glass support: synthesis of a 43-nucleotide sequence similar to the 3'-half molecule of an Escherichia coli formylmethionine tRNA

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